Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP58496.RAwG1wsc7WjbKsSWOjRQBj8aee1_Om6z-ghm7AjHoTErI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP58496.RAwG1wsc7WjbKsSWOjRQBj8aee1_Om6z-ghm7AjHoTErI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP58496.RAwG1wsc7WjbKsSWOjRQBj8aee1_Om6z-ghm7AjHoTErI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP58496.RAwG1wsc7WjbKsSWOjRQBj8aee1_Om6z-ghm7AjHoTErI130_provenance.
- NP58496.RAwG1wsc7WjbKsSWOjRQBj8aee1_Om6z-ghm7AjHoTErI130_assertion wasGeneratedBy ECO_0000203 NP58496.RAwG1wsc7WjbKsSWOjRQBj8aee1_Om6z-ghm7AjHoTErI130_provenance.
- NP58496.RAwG1wsc7WjbKsSWOjRQBj8aee1_Om6z-ghm7AjHoTErI130_assertion wasDerivedFrom gad-20130706 NP58496.RAwG1wsc7WjbKsSWOjRQBj8aee1_Om6z-ghm7AjHoTErI130_provenance.
- NP58496.RAwG1wsc7WjbKsSWOjRQBj8aee1_Om6z-ghm7AjHoTErI130_assertion SIO_000772 15292302 NP58496.RAwG1wsc7WjbKsSWOjRQBj8aee1_Om6z-ghm7AjHoTErI130_provenance.
- NP58496.RAwG1wsc7WjbKsSWOjRQBj8aee1_Om6z-ghm7AjHoTErI130_assertion evidence source_evidence_literature NP58496.RAwG1wsc7WjbKsSWOjRQBj8aee1_Om6z-ghm7AjHoTErI130_provenance.
- NP58496.RAwG1wsc7WjbKsSWOjRQBj8aee1_Om6z-ghm7AjHoTErI130_assertion description "[In summary, linkage of genetic variations of the OPG gene at positions 950 and 1181 may confer an increased risk of CAD in Caucasian men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58496.RAwG1wsc7WjbKsSWOjRQBj8aee1_Om6z-ghm7AjHoTErI130_provenance.
- gad-20130706 importedOn "2013-07-06" NP58496.RAwG1wsc7WjbKsSWOjRQBj8aee1_Om6z-ghm7AjHoTErI130_provenance.